Heavy Rare Earth Research Articles

Superconductivity of thulium substituted clathrate hexahydrides at moderate pressure

Due to the BCS theory, hydrogen, the lightest element, would be the prospect of room-temperature superconductor after metallization, but because of the difficulty of the hydrogen metallization, the theory about hydrogen pre-compression was proposed that the hydrogen-rich compounds could be a great option for the high Tc superconductors. The superior properties of TmH6, YbH6 and LuH6 indicated the magnificent potential of heavy rare earth elements for low-pressure stability. Here, we designed XTmH12 (X = Y, Yb, Lu, and La) to obtain higher Tc while maintaining low pressure stability. Most prominently, YbTmH12 can stabilize at a pressure of 60 GPa. Compared with binary TmH6 hydride, its Tc was increased to 48 K. The results provide an effective method for the rational design of moderate pressure stabilized hydride superconductors.

Age and petrogenesis of ore-bearing porphyry from the Houyu Mo-polymetallic deposit, central North China Craton

Porphyry-related molybdenum deposits formed within the plate's interior are unique, yet the understanding of the magmatic hydrothermal Mo system remains limited. Houyu is a typical porphyry-related Mo-polymetallic deposit situated in the inner region of the North China Craton (NCC). The ore bodies are found in Archean biotite plagioclase gneiss and diorite, followed by Early Cretaceous quartz porphyry, granite porphyry, and brecciated porphyry. Zircon U-Pb dating reveals that the biotite plagioclase gneiss, quartz porphyry, and granite porphyry were formed at 2499.2 ± 7.8 Ma, 135.19 ± 0.67 Ma, and 137.65 ± 0.84 Ma, respectively. Molybdenite Re-Os dating indicates a mean age of 134.94 ± 0.76 Ma and an isochron age of 134.7 ± 1.5 Ma, linking the Mo-polymetallic mineralization closely to the Early Cretaceous porphyry. The Houyu Cretaceous porphyry exhibits enrichment in light rare earth elements (LREEs), depletion in heavy rare earth elements (HREEs), and distinct positive Eu anomalies. Additionally, they are enriched in fluid-mobile large-ion-lithophile elements (LILEs) and significantly depleted in high-field-strength elements (HFSEs). These geochemical attributes suggest that the Cretaceous porphyry belongs to I-type adakitic granites. All samples exhibit consistently negative εNd(t) values ranging from −15.76 to −14.87 and εHf(t) values between −20.69 and −14.78, along with restricted 206Pb/204Pb (16.557–16.663), 207Pb/204Pb (15.262–15.300), and 208Pb/204Pb (36.601–36.747) ratios, indicating that they were derived from an ancient thickened lower continental crust (LCC). The Cretaceous magmatism and mineralization of the Houyu Mo-polymetallic deposit could be closely linked to the lithospheric thinning and destruction of the NCC triggered by the Paleo-Pacific or Izanagi Plate.

Recovery of Rare Earth Elements from Ion-Adsorption Deposits Using Electrokinetic Technology: The Soil Conductivity Mechanism Study

Rare earth elements (REEs) are essential raw materials for modern industries but mining them has caused severe environmental issues, particularly the recovery of heavy REEs (HREEs) from ion-adsorption deposits (IADs). Very recently, an emerging technology, electrokinetic mining (EKM), has been proposed for the green and efficient recovery of REEs from IADs. However, the conduction mechanism of the weathering crust soil, which is also a prerequisite for EKM, remains unclear, making the EKM process unpredictable. Here, we systematically investigated the conductivity of weathering crust soil in the presence of light REEs (LREEs, i.e., La3+ and Sm3+) and HREEs (Er3+ and Y3+), respectively. Results suggested that the voltage was dynamically and spatially redistributed by the movement of REEs and water during EKM, and the conventional assumption of the linear distribution of voltage leads to an inaccurate description of soil voltage. We proposed an improved Archie’s equation by coupling the mechanisms of liquid phase and solid-liquid interface conduction, which can predict soil conductivity more precisely. Moreover, the extended Archie’s equation is able to recalculate the voltage distribution at distinct times and spaces well during EKM. More importantly, the water content in field-scale weathered-crust soils can be retrieved by the newly proposed Archie’s equation, which helps optimize the leaching wells and improve the recovery rate of REE. This study focuses on the conduction mechanism of weathering crust soil, which provides a theoretical basis for better use of the EKM technology and promotes mining efficiency fundamentally.

Strategic grain boundary diffusion process for high-performance Ce-containing sintered Nd-Fe-B magnets

Sintered Nd-Fe-B magnets are an important driver of green technology, and the grain boundary diffusion process (GBDP) has become the most economically efficient method to improve the overall magnetic properties of sintered Nd-Fe-B magnets. In the work, to further reduce the utilization cost of sintered Nd-Fe-B permanent magnets with high performance, the strategic GBDP was explored based on the demagnetization characteristics of Nd-Fe-B permanent magnet materials in motors. The peculiar fact about the process was that the diffusion source was deposited on a part of the c-plane, that is, the strategic selected area grain boundary diffusion process (S-SAGBDP). With the objective of addressing the edge demagnetization, the diffusion source was initially deposited only at the edges of the c-plane. Despite the overall magnetic properties and temperature coefficients of the diffused magnet were significantly enhanced, the serious deteriorations of squareness and surface magnetic field were particularly worrying. Consequently, the central area of the magnet was simultaneously strengthened. The squareness and demagnetization property of the magnet after S-SAGBDP were greatly improved, and the amount of heavy rare earths was reduced by 25%. The above work clearly illustrates the practical value of S-SAGBDP, which is helpful to develop the cost-effective and commercial-grade sintered Nd-Fe-B magnets.

Electro-assisted sorption behavior and mechanism of low-concentration rare earth elements on carbon based materials

With increasing demands for rare earth elements (REEs) in high-tech and futuristic applications, developing efficient methods for recovering low-concentration REEs is necessary. Here, electro-assisted sorption of low-concentration REEs, La(III), Gd(III) and Y(III) (as symbol of light, medium, and heavy REEs) on carbon-based materials, activated carbon (AC), graphene, and graphite by a facile method was reported. Recovery of La(III), Gd(III) and Y(III) could reach ∼100 % under low-concentration condition where the maximum adsorption capacity was up to 342.38 mg/(g·dm2). Variants including applied voltage, electrodes-distance, pH, impurities, and concentration were considered to study the effects on REEs recovery. Interestingly, adsorption capacity and recovery under low voltage were respectively almost 20 and 14 folds than that without voltage, because voltage promoted REEs transfer and strengthened electrostatic interaction between electrodes and REEs. The mechanism for enhancing REEs recovery on carbon-based electrodes was resulted from high electric double layer (EDL) capacitance and low charge transfer resistance. Total desorption of REEs from electrodes could be quickly realized using NH4Cl or HCl solution. Overall, the study gave a new insight of low-concentration REEs recovery using carbon-based materials, and provided an efficient route using electric method with porous materials for REEs recovery.

Nature of ree accumulation in clayey interlayers and coals in Karaganda coal basin

It is the first completed complex mineralogical and geological research of REE (Y, La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu) in the coals of Karaganda coal basin in Central Kazakhstan. This paper presents the results of the research of REE (from lanthanum to lutetium and Y) distribution in 85 samples of coal and clayey interlayers of stratum k7 of Karaganda coal basin in the faces of Saranskaya, T.Kuzembayev, Aktasskaya mines. The ultimate composition of clayey interlayer and coal samples was analyzed by the methods of inductively coupled plasma optical emission spectroscopy and inductively coupled plasma mass spectrometry (ICP-OES and ICP-MS). Research of the lateral and vertical discontinuity of the total REE concentration has indicated the presence of mixed types of REE distribution in coals, which supposes various forms of REE migration and different mobility of heavy and light lanthanides within the hypergenesis zone. The established lanthanum-ytterbium (La/Yb) ratio in the coal, which is normalized to UCC and equals La/Yb<1, relates to the coals with Н type of REE distribution, and the one that equals La/Yb>1 and normalized to chondrite belongs to the coals with L type of REE distribution, which allows making conclusions on the presence of independent sources and different mechanisms of REE accumulation in the sediments of Karaganda coal basin. It is also established that the La/Yb ratio grows from coals to clayey interlayers, which indicates a predominantly clastogenic mechanism of REE input to the coals. The prevailing mineral form of the REE in the coal and clayey interlayer samples from the Karaganda coal basin is light lanthanide phosphates. Sparry crystals with CeLaNdPO composition were found in the coal and clayey interlayer samples. It was established that xenotime is the main deportment for Y in many coals.

Geochemical behavior of rare earth elements in agricultural soils along the Syr Darya River within the Aral Sea Basin.

The widespread use of rare earth elements (REEs) across various industries makes them a new type of pollutant. Additionally, REEs are powerful indicators of geochemical processes. As one of the two main rivers in the Aral Sea, identifying the geochemical behavior of REEs in agricultural soils of the Syr Darya River is of great significance for subsequent indicative studies. In this study, the geochemical characteristics, influencing factors, and potential application significance of REEs in agricultural soils from three sampling areas along the Syr Darya River were analyzed using soil geography and elemental geochemical analyses. The results showed that the highest total concentration of REEs in the agricultural soil was in Area I, with a mean value of 142.49μg/g, followed by Area III with a mean value of 124.56μg/g, and the lowest concentration was in Area II with a mean value of 122.48μg/g. The agricultural soils in the three regions were enriched in light rare earth elements (LREEs), with mean L/H values of 10.54, 10.13, and 10.24, respectively. The differentiation between light and heavy rare earth elements (HREEs) was also high. The concentration of REEs in agricultural soil along the Syr Darya River was primarily influenced by minerals such as monazite and zircon, rather than human activities (the pollution index of all REEs was less than 1.5). The relationship between Sm and Gd can differentiate soils impacted by agricultural activities from natural background soils. The results of this study can serve as a basis for indicative studies of REEs in Central Asia.

Tectono-metamorphic evolution of the Central Bundelkhand Craton, India from geochemistry and bulk composition modelling of amphibolite enclaves

The Bundelkhand Craton (BuC) represents a significant Archean terrane within the northern Indian Craton and yet its tectono-metamorphic evolutionary history remains relatively understudied. Our investigation involves detailed petrography, geochemistry, and bulk composition modeling of both garnet-bearing and garnet-absent amphibolites with a two-fold objective: (i) to constrain the protolithic nature and tectonic settings involved in the genesis of these rocks, and (ii) to propose a tectono-metamorphic evolutionary history for the BuC. The BuC amphibolites originate from basalt and andesitic-basalt protoliths. Their trace element compositions reveal negative anomalies in Nb, Ta, and Ti, while their rare earth element (REE) normalized patterns indicate enrichment in light REEs over heavy REEs. The basaltic protolith is interpreted to have formed during orogeny in a compressional tectonic regime at the active margins of island arcs in a subduction-related setting. This interpretation is supported by various discrimination plots for amphibolites, such as Nb/Th vs Zr/Nb, Zr vs Zr/Y, and Th/Nb vs Ce/Nb, as well as high Th/Yb and low Nb/Yb contents— all of which suggest an island arc setting influenced by subduction. These amphibolites have undergone three distinct phases of metamorphism, as evidenced by petrography, mineral chemistry, and bulk composition modeling. This interpretation is further supported by geochemical discrimination diagrams which indicate that a subduction tectonic setting was active during peak metamorphism. During the pre-peak phase, the garnet-bearing amphibolites experienced pressure and temperature conditions ranging from 6.25 to 6.5 kbar and 580 to 590ºC, while the garnet-absent amphibolites underwent conditions from 5.0 to 5.8 kbar and 400 to 450ºC. Peak metamorphism was observed at pressures ranging from 6.8 to 7.4 kbar and temperatures from 760 to 805ºC for the garnet-bearing amphibolites, and at pressures from 7.0 to 7.4 kbar and temperatures from 785 to 810ºC for the garnet-absent amphibolites. The metamorphic retrograde conditions for the garnet-bearing amphibolites are defined by P-T conditions ranging from 4.45 to 4.75 kbar and 585 to 615ºC, while for the garnet-absent amphibolites, it ranges from 3.1 to 4.0 kbar and 620 to 710ºC. The mineral assemblages and P-T conditions delineate a clockwise P-T path for both, garnet-bearing and garnet-absent amphibolites from the Babina and Mauranipur regions. This suggests that the rocks underwent a burial process amid subduction tectonic settings in an arc-related environment, followed by a decompression stage that brought them to the surface.

Machine learning models to predict rare earth elements distribution in Tethyan phosphate ore deposits: Geochemical and depositional environment implications

The global market for rare earth elements (REE) is growing rapidly, driven by rising demand and limited production sources, prompting interest in recovering REE from secondary sources such as phosphate deposits. The Tethyan belt, extending across North Africa and the Middle East contains substantial Upper Cretaceous to Eocene REE-rich phosphorite deposits but with limited geochemical data available. This study provides a novel machine-learning (ML) method to predict REE contents in these deposits and verify a useful geochemical classification based on the concentrations of nine major element oxides. Four ML models are developed to achieve this: eXtreme Gradient Boosting (XGBoost), Random Forest (RF), Support Vector Regression (SVR), and Decision Tree (DT). The datasets are divided geochemically into oxic and sub-oxic patterns and these are evaluated with the ML models separately and in combination to accurately predict light REE (LREE), heavy REE (HREE), and total REE contents (∑REE). For the oxic pattern dataset, Fe2O3 and K2O exhibit the highest feature importance consistent with a glauconite influence. For the sub-oxic pattern dataset, MnO and SiO2 exhibit the highest feature importance consistent with high terrigenous inputs (MnO), and silicification. The ML results support the importance of the local deposition environment in determining REE distributions in these deposits. Paleogeography, ocean-margin tectonics, sea-level oscillations, and marine currents exert influence on the local depositional environments. The eXtreme Gradient Boosting model generates the lowest REE prediction errors for all the datasets evaluated.

Influence of Organic Matter Thermal Maturity on Rare Earth Element Distribution: A Study of Middle Devonian Black Shales from the Appalachian Basin, USA

This study focuses on understanding the association of rare earth elements (REE; lanthanides + yttrium + scandium) with organic matter from the Middle Devonian black shales of the Appalachian Basin. Developing a better understanding of the role of organic matter (OM) and thermal maturity in REE partitioning may help improve current geochemical models of REE enrichment in a wide range of black shales. We studied relationships between whole rock REE content and total organic carbon (TOC) and compared the correlations with a suite of global oil shales that contain TOC as high as 60 wt.%. The sequential leaching of the Appalachian shale samples was conducted to evaluate the REE content associated with carbonates, Fe–Mn oxyhydroxides, sulfides, and organics. Finally, the residue from the leaching experiment was analyzed to assess the mineralogical changes and REE extraction efficiency. Our results show that heavier REE (HREE) have a positive correlation with TOC in our Appalachian core samples. However, data from the global oil shales display an opposite trend. We propose that although TOC controls REE enrichment, thermal maturation likely plays a critical role in HREE partitioning into refractory organic phases, such as pyrobitumen. The REE inventory from a core in the Appalachian Basin shows that (1) the total REE ranges between 180 and 270 ppm and the OM-rich samples tend to contain more REE than the calcareous shales; (2) there is a relatively higher abundance of middle REE (MREE) to HREE than lighter REE (LREE); (3) there is a disproportionate increase in Y and Tb with TOC likely due to the rocks being over-mature; and (4) the REE extraction demonstrates that although the OM has higher HREE concentration, the organic leachates contain more LREE, suggesting it is more challenging to extract HREE from OM than using traditional leaching techniques.

Petrogenesis of Miocene volcanism in the Central Anatolia: Geochemical, isotopic and geochronological evidence

This paper presents the first 40Ar/39Ar age data, new bulk-rock major-trace element compositions and NdSr isotope geochemistry, combined with detailed geological mapping of Galatia Volcanic Province (GVP) in the northwest Central Anatolia (Turkey). Here, there are voluminous extrusive rocks in a wide compositional range: a basalt, andesite and trachyte suite, and their pyroclastic equivalents. 40Ar/39Ar dating of two whole-rock samples from the GVP yielded plateau ages of 21.76 ± 0.8 Ma and 20.97 ± 0.5 Ma, constrain the volcanic activity at ca. 21 Ma (Aquitanian). The samples show by sub-parallel light rare earth element (LREE)-enrichment and relatively flat heavy rare earth element (HREE) patterns and moderate fractionation [average (La/Yb)N = 13.5]. Their initial 87/86Sr values vary between 0.704619 and 0.704998, while initial 143/144Nd values lie between 0.512673 and 0.512755. Integration of the geochemical and geochronological with geological data we propose that the volcanic rocks in the northern area of GVP with calc-alkaline affinity were produced by a lithospheric mantle magma in an extensional setting.

Nephrite from Xinjiang Qiemo Margou Deposit: Gemological and Geochemical Insights

The nephrite belt in the Altun Mountain–Western Kunlun Mountain region, which extends about 1300 km in Xinjiang, NW China, is the largest nephrite deposit in the world. The Qiemo region in the Altun Mountains is a crucial nephrite-producing area in China, with demonstrated substantial prospects for future exploration. While existing research has extensively investigated secondary nephrite deposits in the Karakash River and native black nephrite deposits in Guangxi Dahua, a comprehensive investigation of black nephrite from original deposits in Xinjiang is lacking. Margou black-toned nephrite was recently found in primary deposits in Qiemo County, Xinjiang; this makes in-depth research on the characteristics of this mine necessary. A number of technical analytical methods such as polarizing microscopy, Ultra-Deep Three-Dimensional Microscope, electron microprobe, back-scattered electron image analysis, X-ray fluorescence, and inductively coupled plasma mass spectrometry were employed for this research. An experimental test was conducted to elucidate the chemical and mineralogical composition, further clarifying the genetic types of the black and black cyan nephrite from the Margou deposit in Qiemo, Xinjiang. The results reveal that the nephrite is mainly composed of tremolite–actinolite, characterized by Mg/(Mg + Fe2+) ratios ranging from 0.86 to 1.0. Minor minerals include diopside, epidote, pargasite, apatite, zircon, pyrite, and magnetite. Bulk-rock rare earth element (REE) patterns exhibit distinctive features, such as negative Eu anomalies (δEu = 0.00–0.17), decreasing light REEs, a relatively flat distribution of heavy REEs, and low total REE concentrations (1.6–38.9 μg/g); furthermore, the Cr (6–21 μg/g) and Ni (2.5–4.5 μg/g) contents are remarkably low. The magmatic influence of granite appears to be a fundamental factor in the genesis of the magnesian skarn hosting Margou nephrite. The distinctive black and black cyan colors are attributed to heightened iron content, mainly associated with FeO (0.08~6.29 wt.%). Analyses of the chemical composition allow Margou nephrite to be classified as typical of magnesian skarn deposits.

Bioleaching ion-unexchangeable rare earth in ion-adsorption type rare earth waste tailing

Ion-adsorption type rare earth ores (IREO) in China serve as the primary source of medium and heavy rare earth globally. With the rapidly growing demand for rare earth elements (REEs) and the dwindling supply of premium IREO, enhancing the recovery of REEs, especially the ion-unexchangeable REEs with ultra-low content and ambiguous speciation from IREO or its tailing, has become a critical trend and challenge. This study identified the occurrences of ion-unexchangeable REEs, primarily detected in Fe-enriched minerals, xenotime, and monazite of IREO using TESCAN integrated mineral analyzer (TIMA) and laser ablation inductively coupled plasma mass spectrometer (LA-ICP-MS) analysis. To extract these elusive REEs, a bioleaching technique utilizing Aspergillus niger (A. niger) metabolites was proposed, achieving a leaching yield of 31.4 wt%. Complementary sequential chemical extraction methods (SCEM), X-ray photoelectron spectroscopy (XPS), and density functional theory (DFT) calculations further elucidate the underlying mechanism, involving the carboxylic acid produced by the metabolic process of microbes that dissolves goethite by disrupting FeO bonds and liberating REEs, which complexed with carboxylate (RCOO), to promote further dissolution. This work offers insight into enhancing the recovery of ion-unexchangeable REEs from IREO or its tailing, paving the way for sustainable and efficient rare earth mining practices.

Effect of Fractionation Columns on the Elution of Rare Earth Elements Recovered from Acid Mine Drainage

Rare earth elements (REE) can be found in expressive contents in different secondary sources, such as acid mine drainage (AMD). This work evaluated separation of light and heavy rare earth elements (REE) from an acid mine drainage (AMD) generated in a former uranium mine in Brazil by using ion exchange. This AMD presents pH 3.50, total REE content of 97 mg L−1 and 1.3 g L−1 of sulfate and was used in the REE loading experiments. Loading experiments were carried out in columns using a commercial strong acid cation (SAC) exchange resin. Elution was performed with 0.01 mol L−1 NH4EDTA in systems with one, two and three columns. Regarding the loading step, the resin presented a total loading capacity of 0.58 mmol g−1. The resin proved to be more selective for light REE with adsorption efficiency of 78% and 48% for heavy REE. Regarding elution, high efficiencies between 90 and 100% were achieved for REE. The final REE solution is approximately 10 times more concentrated in the liquor related to the acid mine water. Better fractionation results were achieved for the system with three columns. Although the complete separation of the REE into pure elements was not possible, two distinct fractions of heavy and light REE could be obtained, and La was completely separated from the other REE. In order to improve fractionation and separate the REE into individual ones, the concentrated fractions can proceed to subsequent ion exchange systems.

Neoarchean high-Mg basalt and rhyolite bimodal complex in the Yinshan Block, North China Craton: Petrogenesis and tectonic implications

Plate tectonics plays an important role in Earth’s evolution, but it is a difficult and controversial issue to trace the operation of plate tectonics in the Archean. Calc-alkaline magmas are a diagnostic feature of modern subduction-related magmatism and thus identification of Archean subduction-related calc-alkaline magmas is crucial for understanding when Archean plate tectonics operated. Here we present zircon U-Pb, whole-rock geochemical and Sr-Nd isotopic data for a metamorphosed Neoarchean calc-alkaline bimodal volcanic complex from the Yinshan Block, the North China Craton. Zircon U-Pb dating results indicate that these meta-volcanic rocks were erupted in the late Neoarchean (∼2570 Ma). Its mafic unit is characterized by high contents of K2O (0.68–4.20 wt%), MgO (Mg# = 62.0-73.4), Cr (332-904 ppm), Ni (105-269 ppm), and is enriched in light rare earth elements (REEs), but depleted in heavy REEs and Nb, Ta and Ti. These geochemical features are similar to those of high-Mg basalts in the Phanerozoic arc setting. They have positive εNd(t) values (+1.3 to + 2.4), indicating that they were derived from the depleted mantle wedge. The felsic unit has variable K2O content (1.42–4.95 wt%) and K2O/Na2O ratios of 0.23–1.36 with positive εNd(t) values (+0.7 to + 3.1). They show characteristics of modern adakites with high Sr/Y and LaN/YbN ratios, suggesting that they were generated by partial melting of the thickened juvenile mafic lower crust. We conclude that the studied Neeoarchean bimodal meta-volcanic complex was formed during subduction-zone retreating and root delamination in a Neoarchean arc. Our results further indicate that plate tectonics had already operated in the Neoarchean in the Yinshan Block.

Rare Earth Elements in Shells of Black Sea Molluscs: Anomalies and Biogeochemical Implications

Rare earth elements (REE) are a class of increasingly used high-tech product components and new emerging environmental pollutants, which are accumulated, in particular, in marine biota. In this study, REE contents were estimated in shells of several molluscs common in the Black Sea. The summed REE contents in mollusc shells decreased in the following order of species: Magallana gigas = Anadara kagoshimensis > Flexopecten glaber ponticus ≥ Rapana venosa > Mytilus galloprovincialis, ranging from 0.46 to 1.9 mg·kg−1. Canonical analysis of principal coordinates allowed for the correct identification of species based on the REE composition in no fewer than 67% of the samples. The mollusc shells were anomalously enriched in Sc, Y, La, Eu and Tb, most likely due to anthropogenic contamination. The Y/Ho ratios in all samples were represented by two fit values: 23.2 (chondritic) and 67.6 (superchondritic, mainly associated with A. kagoshimensis). A new universal relationship linking the contents of three light and heavy REE in Black Sea mollusc shells was proposed: Ce0.3 Er0.7/Yb = 2.00 ± 0.46 (mean ± standard deviation).

Enhancement of the magnetic property of Nd-Fe-B sintered magnets through novel powder rounding modification

Two types of sintered Nd-Fe-B magnets were fabricated by the process of powder metallurgy technology through two different powder preparation processes i.e., conventional powder preparation process and novel powder rounding modification. The microstructure, composition and properties of the two type powders have been studied including the particle size distributions and flowabilities. Furthermore, magnetic properties, microstructure and alignment degree of the magnets prepared by the corresponding powder also have been investigated. The novel powder rounding modification rounds the sharp edges and corners of the particles compared to the conventional powder preparation process, thereby reducing friction between the particles and improving flowability of the powder. As a result, the alignment degree of the sintered magnet is enhanced, which contribute to the improvement of the remanence and the energy product density. The powder that experienced rounding process changed the distribution of RE (rare earth)-rich particles, causing tiny RE-rich particles to adhere around the main phase particles, facilitating the compact of bulk during liquid-phase sintering process and achieving uniform distribution of RE-rich phases around the Nd2Fe14B main phase, resulting in increasing the magnet density and coercivity. As a consequence, we have produced the magnet with Br = 1.43 T, Hcj = 1049 kA/m and (BH)max = 393.2 kJ/m3, which is fully superior to conventional magnet with Br = 1.41 T, Hcj = 969 kA/m and (BH)max = 383.7 kJ/m3 by adopting powder rounding process. This indicates that the novel powder rounding modification is an efficient approach for synchronous improvement of magnetic performance of sintered Nd-Fe-B without any heavy rare earth elements.

RARE-EARTH elements in the topsoils of a Russian industrial city: Sources and human health risk assessment

Research on rare-earth elements (REEs) in urban soils of Russian industrial cities is extremely limited. This study investigates the potential sources and human health risks of REEs contained in the topsoils of the industrial Russian city of Chelyabinsk. The study also takes into account natural sources of REE as the city is located on the border of granites (Urals) and sedimentary rocks (Western Siberia). We analyzed the concentration and distribution of REEs in the soils of four types of locations: residential courtyards, city parks, roadsides, and industrial locations. The total REE concentrations ranged from 44 to 255 mg/kg, with average concentrations of 140, 124, 113 and 89 mg/kg in the courtyards, roadsides, industrial location and city parks, respectively. The REE content in courtyard soils could be influenced by poor cleaning of fallen leaves. The ratios of light REE (LREE) to heavy REE (HREE) ranged from 9.5 to 10.1, revealing an obvious fractionation between them. The fractionation of LREE and HREE, and the REE/ES (European Shale) pattern showed that REE accumulation in Chelyabinsk soils has been disturbed by human activities. It was shown that the dust from industrial emissions was the main anthropogenic source of REE accumulation in urban soil. The largest amounts of REEs are emitted from an electrometallurgical plant and zinc production plant. Fortunately, the estimated daily intakes of REE from soils for children and adults were well below the safety thresholds. At the same time, in order to prevent social tension and reduce the anthropogenic load on the urban area, it is recommended to use phytoremediation technologies, smart landscaping of industrial and residential areas, more thorough cleaning of fallen leaves and road dust. It is also recommended to move the most dangerous production processes outside the urban area.

Garnet geochronology, major and trace element geochemistry of the Huanggangliang Fe-Sn polymetallic deposit, NE China

Cu-Fe (Au), W-Sn (Mo), Pb-Zn (Ag) and other element assemblages are common in many skarn deposits, but examples of Fe and Sn coexistence in nature are relatively rare. The Huanggangliang deposit in the southern Great Xing'an Range is the largest Fe-Sn polymetallic deposit in northern China, and there are five main mining areas (SK Ⅰ–SK Ⅴ) distributed along a SW–NE trend. SK Ⅰ and SK Ⅲ are the two larger mining areas in the Huanggangliang deposit, and their mineral assemblages and wall-rocks are significantly different: cassiterite and metal sulfides are duncommon in SK Ⅰ (andesite), while they are widely distributed in SK Ⅲ (marble). Garnet is widely distributed in SK Ⅰ and SK Ⅲ mining areas, and provides a good opportunity to explore the mechanism of Fe-Sn assemblage differentiation. Three types of garnet are distinguishable (Grt 1, Grt 2 and Grt 3) based on their mineral associations, textures and locations, and they mainly belong to the andradite-grossular solid solution series. The LA–ICP–MS U-Pb ages of the garnets from SK Ⅰ and SK Ⅲ are 136.0 ± 1.2 Ma (n = 25, MSWD = 1.9) and 136.2 ± 2.6 Ma (n = 37, MSWD = 1.8), respectively, suggesting that magmatic-hydrothermal activity in these two mining areas began at the same time. Grt 1 (located deep in SK Ⅰ and SK Ⅲ) and Grt 2 (located shallowly in SK Ⅰ) are mainly andradite, while Grt 3 (located shallowly in SK Ⅲ) is mainly grossular. They are all enriched in high field strength elements (HFSEs) and depleted in large ion lithophile elements (LILEs), and their REE patterns are enriched in light rare earth elements (LREEs) and depleted in heavy rare earth elements (HREEs). However, Grt Ⅰ-1a and 1b (deep garnets in SK Ⅰ) exhibit obvious positive Eu anomalies, while the other garnet types exhibit negative or no obvious Eu anomalies. Additionally, Grt 3 has high contents of V, Sn, U, Th, Zn and Y, and low contents of W and Mo. This pattern implies that the garnets in deep SK Ⅰ may have formed under oxidizing conditions with high temperatures, high oxygen fugacity (fO2) and weak acidity, while the garnets in shallow SK Ⅲ formed under reducing conditions with moderate temperatures, moderate fO2 and near-neutral pH. The garnets in shallow SK Ⅰ and deep SK Ⅲ may have formed under weak oxidation–reduction conditions at moderate to high temperatures, moderate fO2 and weakly acidic to neutral pH conditions. Our newly reported field geological, mineralogical, and geochemical data from garnet suggest that the ore-forming fluids of the Huanggangliang were magmatic-hydrothermal fluids mixed with slightly acidic external fluids, chloride complexes may have been the main transport ligands of REEs. The metallogenic environment may be an important factor leading to the difference of mineral assemblages in the Huanggangliang deposit.

Geochemical characteristics, hazards impact assessment and radiogenic heat production of the alkaline rocks.

This study primarily investigates the natural radioactivity level in alkaline rocks collected from the Wadi El-Dib ring complex (WDRC) in North Eastern Desert of Egypt, and assesses potential health risks associated with their use as decorative building materials. The work was accomplished using a high-purity germanium detector as well as ICP-MS and ICP-AES techniques. The WDRC composed essentially of trachyte, quartz syenite, granite and syenite. Geochemically, these rocks contain high SiO2 and alkalis with metaluminous to slightly peraluminous features. All rocks contain high concentrations of rare earth elements (∑REEs = 109-1075ppm), with clear enrichment in light REEs compared to heavy REEs [(La/Yb)N = 8.3-25.3. Radiometrically, the concentrations of the natural radioisotopes (238U, 232Th, and 40K) in the studied rock types surpassed the worldwide average values assigned for building materials by UNSCEAR. This elevation of the radioisotope concentration values is due to the presence of supplement minerals such as monazite, zircon, allanite, and rutile. Granites exhibit the highest mean concentrations of 238U (av. 164.24 ± 14.76Bq/kg) and 232Th (av. 214.37 ± 23.33Bq/kg), while trachytes demonstrate the highest 40K (av. 1352.56 ± 65.56Bq/kg) concentrations. In contrast, syenites exhibite the lowest mean concentrations for 238U (av. 54.51 ± 6.81Bq/kg) and 232Th (av. 56.76 ± 6.25Bq/kg), while quartz syenites display the lowest mean concentration of 40K (av. 1144.78 ± 96.19Bq/kg). The radiogenic heat production (RHP) associated with U, Th, and K range between 1.41 to 9.33μW/m3, exceeding the typical crustal mean value of 0.8 to 1.2μW/m3. The radiological parameters and indices evaluating risks of the outdoor and indoor radiation doses due to the investigated rocks were assessed. The results indicated that these rocks meet globally accepted values and safety standards (approved by UNSCEAR, ICRP, and EC) for surface building materials, as well as they underscore the importance of adhering to safety protocols to safeguard workers from radiation exposure within the WDRC area. Ultimately, the data herein provide a valuable database for assessing the compatibility of geochemical data and natural radioactivity level in WDRC rocks. Additionally, it reveals that from the radiological perspective, the investigated rocks are considered safe for use as decorative construction materials.